Pereyra Susana B, Danielo Cristián A, Ponssa Gustavo J, Consigli Javier E, Papa Mariana B, Ghirardi Graciela
Departments of Dermatology and Pathology, Hospital Córdoba, Córdoba, Argentina.
Int J Dermatol. 2007 Sep;46(9):944-6. doi: 10.1111/j.1365-4632.2007.03233.x.
Wade's histoid leprosy is a rare form of multibacillary leprosy with distinctive characteristics which were first described in patients treated with a short course of sulfones. Wade's histoid leprosy may occur as a relapse, in the setting of sulfone resistance, or may present de novo. We report the clinical, histologic, immunologic, and bacteriologic features of three adult male patients with this rare variant of lepromatous leprosy as the initial presentation of the disease, observed in the Dermatology Department of Hospital Córdoba, Córdoba, Argentina between 1999 and 2003. Two of the three patients were from an endemic leprosy area. All patients presented with a number of erythematous to brownish gray, firm but elastic nodules involving mainly the extremities, which responded to treatment for multibacillary leprosy without reactional episodes.
韦德类瘤型麻风是一种罕见的多菌型麻风,具有独特的特征,最初是在用短疗程砜类药物治疗的患者中描述的。韦德类瘤型麻风可能表现为复发,出现在对砜类药物耐药的情况下,也可能是初发。我们报告了1999年至2003年在阿根廷科尔多瓦省科尔多瓦市医院皮肤科观察到的3例成年男性患者的临床、组织学、免疫学和细菌学特征,这些患者以这种罕见的瘤型麻风变异型作为疾病的首发表现。3例患者中有2例来自麻风流行地区。所有患者均出现多处红斑至棕灰色、质地硬但有弹性的结节,主要累及四肢,对多菌型麻风治疗有反应,未出现反应性发作。